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在存在可能的降解产物的情况下,对沙芬酰胺进行稳定性指示分光光度法定量分析。

Stability-indicating spectrophotometric quantification of safinamide in the presence of its possible degradation product.

作者信息

Kamel Ebraam B, El-Abassy Omar M

机构信息

Pharmaceutical Chemistry Department, Faculty of Pharmacy, Egyptian Russian University, Badr City, 11829, Cairo, Egypt.

出版信息

Sci Rep. 2025 Jan 6;15(1):1035. doi: 10.1038/s41598-024-83195-9.

Abstract

In recent times, a truly exquisite pharmaceutical marvel has graced the world of medicine, known as Safinamide (SAF). This opulent creation has been specifically tailored to cater to the needs of individuals afflicted with Parkinson's disease (PD), an esteemed neurological condition renowned for its regal ability to impede motor skills, coordination, and equilibrium. It is highly improbable that degradation products of pharmaceutical components would significantly compromise efficiency and safety of a drug during its shelf life. Pharmaceutical analysis requires a variety of stability tests to be conducted under distinct conditions. As a result, there was an increased need for the development of an analytical methodology capable of reliably separating and quantifying degradants and impurities that might be found in pharmaceuticals. In this study, we have developed two efficient and straightforward spectrophotometric methodologies for the concurrent estimation of SAF and its degradation product (SAF DEG), which is the main acid hydrolysis product. The confirmation of degradation product build-up by the use of several analytical techniques, including infrared spectroscopy (IR), and mass spectrometry (MS) investigations. The present methodologies have been validated for linearity within the concentration range of 5-30 µg/ml for SAF, and 5-15 µg/mL, 2-15 µg/ml for SAF DEG for fourier self-deconvolution (FSD) and dual wavelength (DW) methods, respectively. The originality of these techniques lies in their status as the first stability-indicating spectrophotometric procedures that are both environmentally friendly. Moreover, the process of obtaining pure SAF DEG offers substantial economic benefits by obviating the need to acquire a costly constituent. The use of intelligent techniques was employed to analyze the pharmaceutical dosage form, potentially offering significant advantages to the pharmaceutical industry.

摘要

近年来,一种堪称精妙绝伦的药物奇迹降临医学界,它就是沙芬酰胺(SAF)。这一卓越的发明是专门为满足帕金森病(PD)患者的需求而研制的,帕金森病是一种备受瞩目的神经疾病,以其显著影响运动技能、协调性和平衡能力而闻名。药物成分的降解产物在药品保质期内极不可能对药物的有效性和安全性造成重大损害。药物分析需要在不同条件下进行多种稳定性测试。因此,越来越需要开发一种能够可靠地分离和定量药物中可能存在的降解产物和杂质的分析方法。在本研究中,我们开发了两种高效且简便的分光光度法,用于同时测定SAF及其降解产物(SAF DEG),SAF DEG是主要的酸水解产物。通过使用包括红外光谱(IR)和质谱(MS)研究在内的多种分析技术,对降解产物的积累进行了确认。目前的方法已分别针对傅里叶自去卷积(FSD)法和双波长(DW)法在SAF浓度范围为5 - 30μg/ml以及SAF DEG浓度范围为5 - 15μg/mL、2 - 15μg/ml内进行了线性验证。这些技术的独特之处在于它们是首批既环保又具有稳定性指示作用的分光光度法。此外,获得纯SAF DEG的过程通过无需获取昂贵成分而带来了可观的经济效益。采用智能技术对药物剂型进行分析,可能会给制药行业带来显著优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1a/11704146/a0115c3f2d1e/41598_2024_83195_Fig1_HTML.jpg

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